Package 69367-287-09
Brand: montelukast sodium
Generic: montelukast sodiumPackage Facts
Identity
Package NDC
69367-287-09
Digits Only
6936728709
Product NDC
69367-287
Description
90 TABLET in 1 BOTTLE (69367-287-09)
Marketing
Marketing Status
Brand
montelukast sodium
Generic
montelukast sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1026f850-9f36-346f-e063-6394a90a2373", "openfda": {"upc": ["0369367287050"], "unii": ["U1O3J18SFL"], "rxcui": ["200224"], "spl_set_id": ["c0daaaf3-6717-4a01-e053-2995a90af2d8"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (69367-287-05)", "package_ndc": "69367-287-05", "marketing_start_date": "20210425"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (69367-287-09)", "package_ndc": "69367-287-09", "marketing_start_date": "20210425"}], "brand_name": "Montelukast Sodium", "product_id": "69367-287_1026f850-9f36-346f-e063-6394a90a2373", "dosage_form": "TABLET", "pharm_class": ["Leukotriene Receptor Antagonist [EPC]", "Leukotriene Receptor Antagonists [MoA]"], "product_ndc": "69367-287", "generic_name": "Montelukast Sodium", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Montelukast Sodium", "active_ingredients": [{"name": "MONTELUKAST SODIUM", "strength": "10 mg/1"}], "application_number": "ANDA205683", "marketing_category": "ANDA", "marketing_start_date": "20160530", "listing_expiration_date": "20261231"}